This document discusses drug dosing considerations for obese patients. It notes that obesity is associated with increased risk of diseases like hypertension and diabetes. Obesity can impact drug pharmacokinetics through changes in volume of distribution, metabolism, and elimination. For many drugs, dosing should be based on lean body weight rather than total weight to avoid overdosing. Close monitoring of drug effects is recommended when treating obese patients.
This document discusses drug dosing considerations for obese patients. It notes that obesity is associated with increased risk of diseases like hypertension and diabetes. Obesity can impact drug pharmacokinetics through changes in volume of distribution, metabolism, and elimination. For many drugs, dosing should be based on lean body weight rather than total weight to avoid overdosing. Close monitoring of drug effects is recommended when treating obese patients.
This document discusses drug dosing considerations for obese patients. It notes that obesity is associated with increased risk of diseases like hypertension and diabetes. Obesity can impact drug pharmacokinetics through changes in volume of distribution, metabolism, and elimination. For many drugs, dosing should be based on lean body weight rather than total weight to avoid overdosing. Close monitoring of drug effects is recommended when treating obese patients.
PHARM.D POST BACCALAURATE MANIPAL Drug Dosing in Obesity Obesity BMI> 30 Drug dosing is difficult as there is only limited information is available. It is estimated that by 2010, 40% of the US adult population will be obese. Obesity increases the risk of multiple disease states including hypertension, diabetes mellitus, and coronary artery disease. Calculations
slightly increased lean tissue mass increased cardiac output increased glomerular filtration rate fatty infiltration of liver Phamacokinetics in obesity
Oral availability (F)
Oral availability in obese patients does not appear to
be different from in non-obese patients. Volume of distribution
Hydrophilic drugs : generally no change in Vd. e.g.
lithium. Lipophilic drugs : Increased adipose tissue mass can influence Vd. e.g. aminoglycosides To prevent overdosing in obesity, a dosing weight correction factor of 0.4 is used to account for the altered volume of distribution. Metabolism
Phase 1 reactions unchanged in obesity
Phase 2 reactions increased in obesity.
Eg: Lorazepam, Oxazepam Increased metabolism of this drugs may result in suboptimal concentration. Fatty infiltration of liver may occur in obese patients. Elimination
Renal clearance Glomerular filtration increases in obesity resulting in increased clearance of many renally cleared drugs.
Tubular function i.e. tubular secretion and reabsorption
of some drugs may also be increased in obesity. Estimation of Cr.Cl in Obesity Recommendations
Be aware that obese patients may require dose adjustment
especially for low therapeutic index drugs. Maximum recommended doses should not normally be exceeded. Monitor the effects of medication both clinically and with therapeutic drug monitoring if appropriate, and be prepared to make dose adjustments. Larger loading doses may be required.. Maintenance dose – for most drugs should be based on Lean Body Weight, a weight of approximately Ideal weight + ⅓ X (Total weight – Ideal Weight)
Effects of Juglans Nigra (Black Walnut) and Urtica Dioica (Nettle Leaf) On Lipid Profile of Thiamazole Induced Hypothyroidism in Obese Wistar Albino Rats